A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018188



Internal ID19107405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:9798243..9821783hg38UCSC Ensembl
Innerchr9:9798243..9821783hg19UCSC Ensembl
Innerchr9:9788243..9811783hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3823541
hg1923541
hg1823541
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7398n100
Supporting Variantsnssv3689143
Samples
Known GenesPTPRD
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018188
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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